United States · FDA National Drug Code directory
Mirtazapine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68788-7251_2090f40c-c357-4520-a4cf-3c5200ac7b2a
- Product NDC
- 68788-7251
- Form
- TABLET, FILM COATED
- Composition / generic term
- Mirtazapine
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180828
- Source listing expiry
- 20271231
Source-listed ingredients
- MIRTAZAPINE — 15 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE (68788-7251-1) · 68788-7251-1
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-7251-3) · 68788-7251-3
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-7251-6) · 68788-7251-6
- 90 TABLET, FILM COATED in 1 BOTTLE (68788-7251-9) · 68788-7251-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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